643745-50-0

Upstream product

• 111-83-1 1-bromo-octane 
• 769-39-1 2,3,5,6-tetraflourophenol 
• 111-87-5 octanol 
• 363-72-4 Pentafluorobenzene 

Downstream Products

• 643745-45-3 Au(C₆F₄OC₈H₁₇)(CNC₆H₄O₂CC₆H₄OC₄H₉) 
• 643745-48-6 Au(C₆F₄OC₈H₁₇)(CNC₆H₄O₂CC₆H₄OC₁₀H₂₁) 
• 643745-49-7 Au(C₆F₄OC₈H₁₇)(CNC₆H₄O₂CC₆H₄OC₁₂H₂₅) 
• 643745-47-5 Au(C₆F₄OC₈H₁₇)(CNC₆H₄O₂CC₆H₄OC₈H₁₇) 
• 643745-46-4 Au(C₆F₄OC₈H₁₇)(CNC₆H₄O₂CC₆H₄OC₆H₁₃) 
• 918414-23-0 [μ-(2,2'-dimethyl-4,4'-diisocyanobiphenyl)(Au(1-octyloxy-2,3,5,6-tetrafluorobenzene(-1H)))2] 
• 918414-19-4 [μ-(2,2'-dichloro-4,4'-diisocyanobiphenyl)(Au(1-octyloxy-2,3,5,6-tetrafluorobenzene(-1H)))2] 
• 918414-15-0 [μ-(4,4'-diisocyanobiphenyl)(Au(1-octyloxy-2,3,5,6-tetrafluorobenzene(-1H)))2] 
• 918414-25-2 [μ-(1,4-diisocyanobenzene)(Au(1-octyloxy-2,3,5,6-tetrafluorobenzene(-1H)))2] 
• 76071-03-9 4-(octyloxy)-2,3,5,6-tetrafluorobenzoic acid 
• 1253824-74-6 4-octyloxy-2,3,5,6-tetrafluoroiodobenzene 

Relevant academic research and scientific papers

Structure and ionic conductivity of liquid crystals having propylene carbonate units

Liquid-crystalline compounds with a perfluorinated aromatic ring as the mesogenic core and a propylene carbonate unit were prepared and mixed with lithium bis(trifluoro-methanesulfonyl)-imide (LiTFSI). The self-assembly was driven by the interaction of th

Selective C4-F bond cleavage/C-O bond formation of polyfluoroarenes with phenols and benzyl alcohols

A facile and efficient SNAr method for the synthesis of unsymmetrical polyfluoroaryl ethers via selective C4-F bond cleavage of pentafluorobenzene is reported. The reaction could proceed smoothly without the requirement of additional metals or ligands, and afford a series of the corresponding products in good to high yields. A wide variety of substituted phenols and alcohols provided 1,2,4,5-tetrafluoropheny ether derivatives in regioselective manner.

Structure-function relationships in liquid-crystalline halogen-bonded complexes

New liquid-crystalline materials were prepared by self-assembly driven by halogen bonding between a range of 4-alkoxystilbazoles, 4-alkyl-, and 4-alkoxy-substituted pyridines as halogen-bonding acceptors, and substituted derivatives of4-iodotetrafluorophenyl as halogen-bonding donors. Despite the fact that the starting materials are not mesomorphic, the dimeric, halogen-bonded complexes obtained exhibited nemetic and SmA phases, depending on the length of the alkylchains present on the components. The modularity of this approach also led to new chiral mesogens starting from non-mesomorphic chiral compounds.

Liquid crystalline organic semiconductor material and organic semiconductor device using same

The present invention provides a novel organic semiconductor material that affords efficient charge transport, under a wider range of conditions, by increasing the temperature stability and expanding the temperature range of the organic semiconductor mate